Characterising heart rhythm abnormalities associated with Xp22.31 deletion
Sign Up to like & getrecommendations! Published in 2022 at "Journal of Medical Genetics"
DOI: 10.1136/jmg-2022-108862
Abstract: Background Genetic deletions at Xp22.31 are associated with the skin condition X linked ichthyosis (XLI), and with a substantially increased risk of atrial fibrillation/flutter (AF), in males. AF is associated with elevated thrombosis, heart failure,… read more here.
Keywords: deletion; xp22 deletion; associated xp22; risk ... See more keywords